Infant Primates Given Vaccines on U.S. Children's Immunization Schedule Develop Biomedical and Behavioral Symptoms of AutismGroundbreaking Research Provides Even More Science Supporting the Theory that Vaccines Can and Do Cause Autism
NIXA, Mo., May 19, 2008 /PRNewswire-USNewswire/ -- A primate model for autism using the U.S. children's immunization schedule was unveiled at the International Meeting For Autism Research (IMFAR) this weekend. The research underscores the critical need for studies into vaccine safety and the immune and mitochondrial dysfunction of autistic children. The National Autism Association (NAA) questions why the government hasn't undertaken these vital studies and why researchers have had to depend on private money to perform this critical science that will surely impact the health of millions of children worldwide.
Using infant macaque monkeys, Dr. Laura Hewitson, Ph.D., described how vaccinated animals, when compared to unvaccinated animals, showed significant neurodevelopmental deficits and "significant associations between specific aberrant social and non-social behaviors, isotope binding, and vaccine exposure."
Researchers also reported, "vaccinated animals exhibited progressively severe chronic active inflammation whereas unexposed animals did not" and found "many significant differences in the GI tissue gene expression profiles between vaccinated and unvaccinated animals." Gastrointestinal issues are a common symptom of children with regressive autism.
NAA calls for the NIH to conduct large scale, non-epidemiological studies into the biomedical symptoms surrounding young children and all vaccines, including those containing the mercury-based preservative thimerosal and other additives like aluminum.
This request for further research echoes that of Dr. Bernadine Healy, Former NIH Director in a CBS interview earlier this week. "I think public health officials have been too quick to dismiss the hypothesis as 'irrational,' without sufficient studies of causation...without studying the population that got sick," Healy said. "I have not seen major studies that focus on 300 kids who got autistic symptoms within a period of a few weeks of the vaccines."
Recently the government's vaccine court conceded the case of Hannah Poling, admitting that vaccines triggered her regression into autism by exacerbating mitochondrial dysfunction. "The recent Poling case and this new research provide further evidence that the CDC has fallen down on their job to protect children from harm. The biomedical research to date suggests that parental reports of regression following vaccination is not only plausible, but likely in certain individuals," said Scott Bono, NAA Chairman. "To date, the CDC has conducted no safety testing on the possible harmful effects of simultaneously administering multiple vaccines to infants, and has steadfastly refused to state a preference for mercury-free vaccines to be given to children and pregnant women. It's time for HHS and Congress to step in and take vaccine safety away from the CDC."
On June 4th, parents of vaccine-injured children will rally for toxin-free immunizations in Washington, DC. For more information about the "Green Our Vaccines" rally or the new primate study visit www.nationalautism.org.
Wendy Fournier (Portsmouth, RI) 401-835-5828
Rita Shreffler (Nixa, MO) 401-632-6452
CONTACT: Wendy Fournier (Portsmouth, RI), +1-401-835-5828, or RitaShreffler (Nixa, MO), +1-401-632-6452, both for National Autism Association
Web site: http://www.nationalautism.org/
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Posted: May 2008
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